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The Journal of Maternal-Fetal & Neonatal Medicine Volume 28, 2015 - Issue 10
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Original Article

Initial experience with non-invasive prenatal testing of cell-free DNA for major chromosomal anomalies in a clinical setting

Carmina ComasFetal Medicine Unit, Department of Obstetrics and Gynecology, Hospital Universitari Quirón Dexeus, Barcelona, SpainCorrespondence[email protected]
,
Mónica EchevarriaFetal Medicine Unit, Department of Obstetrics and Gynecology, Hospital Universitari Quirón Dexeus, Barcelona, Spain
,
M Angeles RodríguezFetal Medicine Unit, Department of Obstetrics and Gynecology, Hospital Universitari Quirón Dexeus, Barcelona, Spain
,
Pilar PratsFetal Medicine Unit, Department of Obstetrics and Gynecology, Hospital Universitari Quirón Dexeus, Barcelona, Spain
,
Ignacio RodríguezFetal Medicine Unit, Department of Obstetrics and Gynecology, Hospital Universitari Quirón Dexeus, Barcelona, Spain
&
Bernat SerraFetal Medicine Unit, Department of Obstetrics and Gynecology, Hospital Universitari Quirón Dexeus, Barcelona, Spain
Pages 1196-1201 | Received 11 Jun 2014, Accepted 20 Jul 2014, Published online: 12 Aug 2014

Citations (13)

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Cechuan Deng, Sau Wai Cheung & Hongqian Liu. (2021) Noninvasive prenatal screening for fetal sex chromosome aneuploidies. Expert Review of Molecular Diagnostics 21:4, pages 405-415.
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Nerea Maiz, Irune Alzola, Emerson J. Murua & Javier Rodríguez Santos. (2016) Cell-free DNA testing after combined test: factors affecting the uptake. The Journal of Maternal-Fetal & Neonatal Medicine 29:21, pages 3558-3562.
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Articles from other publishers (11)

Soojin Kim, Esther L. Finney, Ushasi Naha, Ilina Rosoklija, Kyle S. Honegger, Allison Goetsch Weisman, Jane L. Holl, Courtney Finlayson, Diane Chen & Emilie K. Johnson. (2023) Comparison of web-based information about cell-free DNA prenatal screening: implications for differences of sex development care. Frontiers in Urology 3.
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Zachary Demko, Brittany Prigmore & Peter Benn. (2022) A Critical Evaluation of Validation and Clinical Experience Studies in Non-Invasive Prenatal Testing for Trisomies 21, 18, and 13 and Monosomy X. Journal of Clinical Medicine 11:16, pages 4760.
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Nardhy Gomez-Lopez, Roberto Romero, George Schwenkel, Valeria Garcia-Flores, Bogdan Panaitescu, Aneesha Varrey, Fatime Ayoub, Sonia S. Hassan & Mark Phillippe. (2020) Cell-Free Fetal DNA Increases Prior to Labor at Term and in a Subset of Preterm Births. Reproductive Sciences 27:1, pages 218-232.
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Anne Rummer, Wiebke Sieben, Christoph Mosch, Oliver Assall & Stefan Sauerland. (2019) Nicht invasive Pränataldiagnostik mittels molekulargenetischer Tests (NIPT) zur Erkennung der Trisomien 13, 18 und 21Non-invasive molecular genetic prenatal tests (NIPT) for detection of trisomy 13, 18 and 21. medizinische genetik 31:3, pages 275-282.
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Yoshiteru Noda, Takema Kato, Asuka Kato, Haruki Nishizawa, Jun Miyazaki, Mayuko Ito, Sumire Terasawa, Takao Sekiya, Takuma Fujii & Hiroki Kurahashi. (2018) Potentially effective method for fetal gender determination by noninvasive prenatal testing for X‐linked disease. Congenital Anomalies 59:3, pages 88-92.
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Da Eun Lee, Hyunjin Kim, Jungsun Park, Taegyun Yun, Dong Yoon Park, Minhyoung Kim & Hyun Mee Ryu. (2019) Clinical Validation of Non-Invasive Prenatal Testing for Fetal Common Aneuploidies in 1,055 Korean Pregnant Women: a Single Center Experience. Journal of Korean Medical Science 34:24.
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Mylène Badeau, Carmen Lindsay, Jonatan Blais, Leon Nshimyumukiza, Yemisi Takwoingi, Sylvie Langlois, France Légaré, Yves Giguère, Alexis F Turgeon, William Witteman & François Rousseau. (2017) Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women. Cochrane Database of Systematic Reviews 2017:11.
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Erik Iwarsson, Bo Jacobsson, Jessica Dagerhamn, Thomas Davidson, Eduardo Bernabé & Marianne Heibert Arnlind. (2017) Analysis of cell-free fetal DNA in maternal blood for detection of trisomy 21, 18 and 13 in a general pregnant population and in a high risk population - a systematic review and meta-analysis. Acta Obstetricia et Gynecologica Scandinavica 96:1, pages 7-18.
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Sian Taylor-Phillips, Karoline Freeman, Julia Geppert, Adeola Agbebiyi, Olalekan A Uthman, Jason Madan, Angus Clarke, Siobhan Quenby & Aileen Clarke. (2016) Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis. BMJ Open 6:1, pages e010002.
Crossref
Whitney A. Neufeld-Kaiser, Edith Y. Cheng & Yajuan J. Liu. (2015) Positive predictive value of non-invasive prenatal screening for fetal chromosome disorders using cell-free DNA in maternal serum: independent clinical experience of a tertiary referral center. BMC Medicine 13:1.
Crossref
Gautam N. Allahbadia. (2015) Has Noninvasive Prenatal Testing (NIPT) Come of Age?. The Journal of Obstetrics and Gynecology of India 65:3, pages 141-145.
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